Characterization of neurobehavioral pattern in a zebrafish 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced model: A 96-hour behavioral study

Parkinson’s disease (PD) is the most common brain motor disorder, characterized by a substantial loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc). Motor impairments, such as dyskinesia, bradykinesia, and resting tremors, are the hallmarks of PD. Despite ongoing research, the exact PD pathogenesis remains elusive due to the disease intricacy and difficulty in conducting human studies. Zebrafish (Danio rerio) has emerged as an ideal model for researching PD pathophysiology. Even though 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) has been used to induce PD in zebrafish, behavioural findings are frequently limited to a single time point (24 hours post-injection). In this sense, we aim to demonstrate the effects of MPTP on zebrafish swimming behaviour at multiple time points. We administered a single dosage of MPTP (200μg/g bw) via intraperitoneal injection (i/p) and assessed the locomotor activity and swimming pattern at 0h, 24h, and 96h post-injection through an open field test. Analysis of the behaviour revealed significant reductions in swimming velocity (cm/s) and distance travelled (cm), concurrent with an increase in freezing maintenance (duration and bouts) in zebrafish injected with MPTP. In addition, the MPTP-injected zebrafish exhibited complex swimming patterns, as measured by the turn angle, meander, and angular velocity, and showed abnormal swimming phenotypes, including freezing, looping, and erratic movement. To conclude, MPTP administration into adult zebrafish induced hypolocomotion and elicited motor incoordination. Plus, the effects of MPTP were observable 24 hours after the injection and still detectable 96 hours later. These findings contribute to the understanding of MPTP effects on adult zebrafish, particularly in terms of swimming behaviours, and may pave the way for a better understanding of the establishment of PD animal models in the future.

particularly in terms of swimming behaviours, and may pave the way for a better understanding of the establishment of PD animal models in the future.
swimming behaviour at multiple time points (0h, 24h, and 96h after injection) by assessing the locomotor activity and swimming pattern. We delivered the MPTP to the peritoneal cavity of the zebrafish via intraperitoneal injection (i/p). We then conducted an open field test to statistically compare the swimming behaviours between control (saline-injected) and MPTPinjected zebrafish. Most of the PD research utilizing neurotoxin-induced models aim to develop therapeutic treatments that can potentially relieve PD symptoms. Hence, to avoid potential result misinterpretation due to confounding factors, it is important ensure that the PD model is already sustained and stabilized prior to any therapeutic interventions. Our study sheds light on the initial trend of MPTP effect adult zebrafish, particularly in terms of the swimming behaviour. Findings from this study could pave the way for a better understanding of PD animal models establishment in the future.

Instrumentation
A 31G needle attached to a 0.5ml insulin syringe (U-100 Insulin 0.5ml 31G X 5/16˝, Ter-umo1, Tae Chang Industrial Co., Ltd., Gyeongsangbuk-do, Korea) was used to administer saline and MPTP into zebrafish peritoneal cavity. Realme RMX1851 camera (Shenzen, China) set at 720p resolution and 30fps frame rate was used to record the swimming behaviour of adult zebrafish. Pre-processing of the recorded videos was done using VideoPad Professional version 7.32 (NCH Software Inc., CO, USA) video editor software. Analysis of the recorded videos was done by Noldus EthoVision XT version 11.5 (Noldus Information Technology, Wageningen, The Netherlands) tracking software. Statistical analysis was performed using GraphPad Prism 9.00 for Windows (GraphPad Software, CA, USA).

Zebrafish husbandry
A total of 40 male and female wild-type zebrafish (Danio rerio) aged three to four months old with an average initial body weight of 0.9 ± 0.1g were used in this study. The zebrafish were purchased from a local breeder in Kuantan, Pahang, Malaysia. All zebrafish were housed inside a 10L acrylic fish aquarium sized 58.5 cm (L) x 28.0cm (W) x 36.0cm (H) located at the IIUM Central Research and Animal Facility (CREAM) and given at least 10 days to acclimatize prior to the start of the experiment. Both aquariums (housing and experimental) were filled with filtered facility water and kept at a constant temperature of 26 ± 2˚C, had air bubbles for aeration, and biofilter stones to facilitate the nitrate degradation process. White fluorescence lamps were used to provide illumination with a 14h-light to 10h-darkness cycle, compliant with standard zebrafish care guidelines [20]. The zebrafish were fed three times a day (09:00, 12:00, and 16:00).

Experimental design
Zebrafish were randomly divided into two groups (control and MPTP-injected groups), with each group consisting of 20 fish (n = 20). On the experimental days, zebrafish were fed one hour prior to the start of the procedure. Then, they were injected with either saline or MPTP depending on their assigned group. Swimming behaviour tests were performed at 0h, 24h, and 96h after injection. The initial and final weights (g) of each experimental zebrafish were recorded. Throughout the experimental period, zebrafish were housed individually, each in a 1.5L home tank sized 18.0cm (L) x 11.0cm (W) x 9.5cm (H). The entire experiment took five days to complete, and all zebrafish were sacrificed immediately after the completion of the study. The experimental paradigm of this study was permitted by the Institutional Animal

MPTP treatment
The powdered MPTP was dissolved with saline solution to prepare a 10mg/ml stock solution. MPTP is commonly administered into the adult zebrafish system via i/p injection or delivered directly into the brain through intracerebroventricular injection [21,22]. In our study, we chose to administer the MPTP via i/p injection due to its proven rate of success and recovery as well as affordability [23,24]. Prior to the injection, zebrafish were anesthetized with ice-cold water. One dose of 30μl of working solution containing 200μg MPTP per gram of body weight (200μg/g bw) was intraperitoneally administered into the zebrafish using a 31G needle attached to an insulin syringe (Fig 2). The point of the injection was at the abdominal cavity located posterior to the pelvic girdle, specifically at 45˚to the base of the pelvic fin [23,24]. The injection method was justified by looking for (1) mortality, (2) bleeding at the site of injection, (3) aberrant behaviour post-injection, (4) injection solution leakage, and (5) MPTP effect as critical indicators of injection success [24]. No documented mortality, bleeding, aberrant behaviour, and solution leakage, as well as the significant MPTP effect exhibited by the MPTPinjected group justified the success of the injection method. Control zebrafish were injected with 30μl of saline solution. Immediately after the injection, zebrafish were transferred into a recovery tank treated with anti-bacterial treatment to facilitate wound healing. All zebrafish were monitored upon recovery for any side effects or injuries.

Swimming behaviour test
Recording setup. The recording setup was adapted from Selvaraj et al. [19] and modified where necessary. A 2.5L acrylic tank sized 24.0cm (L) x 13.5cm (W) x 13.5cm (H) was used as an assay tank. The tank was digitally divided into two imaginary zones, the inner IN zone and the outer OUT zone. The IN zone is a rectangular zone measuring 18cm (L) x 7.5 (W) located

PLOS ONE
at the centre of the assay tank while the OUT zone is located between the IN zone and the wall of the assay tank. The tank was placed on a stable surface and filled with filtered facility water until 8cm-height. The entire setup was walled with cardboard boxes and the experiment was conducted in an isolated room to minimize external visual and auditory noises. Illumination was supplied by LED lights. A camera was mounted on top of the tank to capture the top view. The recorded videos were saved in.mp4 format.
Swimming behaviour recording. A swimming behaviour test was performed every day from 0h until 96h post-injection. To minimize variances, the recording was executed at the same time (from 12.00 until 14:00) and in the same room each day. The test was performed on each zebrafish individually. Prior to the test, the zebrafish were acclimatized inside the assay tank for 5-10 minutes to familiarize themselves with the environment. After that, the zebrafish were let to swim in the tank for three minutes and their swimming behaviour was recorded throughout the swimming period. During the recording session, the experimenter monitored the zebrafish only through a monitor screen to prevent experimenter visibility and minimize experimenter effects. After the test, the zebrafish were immediately transferred back to their home tank. The recorded behaviours were analysed using Noldus EthoVision XT version 11.5 tracking software. Each parameter was compared between the control (saline-injected) and MPTP-injected groups.
Behavioural analysis. The swimming behaviour was defined by two measures: locomotor activity and swimming pattern [25]. The locomotor activity was evaluated in terms of swimming velocity (cm/s), total distance travelled (cm), and freezing maintenance (duration (s) and bouts), while the swimming pattern was examined in terms of the frequency and time spent (s)

Statistical analysis
All parameters were analysed statistically through RM two-way ANOVA comparing the control and MPTP-injected groups, with Tukey's multiple comparisons test, as recommended by the statistical software. To ensure that the samples met the assumptions of the statistical approach, a normality test was performed prior to the RM two-way ANOVA. According to the Shapiro Wilk test for normality, both groups were normally distributed for all parameters. Aside from that, the samples met all other assumptions, including having continuous dependent variables, having an adequate sample size (as determined by G � Power software), and having similar relationship between the pairs of experimental conditions (as proven by Mauchly's test). The analysed data were presented as mean. P-values of less than 0.05 (p < 0.05) were considered significant for all statistical analyses.

Effects of MPTP on adult zebrafish swimming behaviour
The alteration in the swimming behaviour of zebrafish after the i/p injection of MPTP neurotoxin was analysed. Several dosages of MPTP were evaluated in pilot experiments to determine the lowest observable effect level of the neurotoxin. 200μg of MPTP per gram body weight of zebrafish (200μg/g bw) elicited practically maximal decreases of general locomotor activity (swimming velocity and distance travelled) (data not shown), and thus, all subsequent investigations were conducted with this dose.
The zebrafish locomotor activity was markedly altered after the i/p injection of MPTP neurotoxin. Specifically, the alteration was already detected by 24h after MPTP injection and remained altered 96h after the injection. The swimming velocity of MPTP-injected zebrafish was decreased by 30% 24h after the injection and remained low on the 96th hour after the injection ( Fig 3A). In terms of the distance travelled, the MPTP-injected zebrafish swam 30% shorter distances 24h and 96h after injection (Figs 3B and 4). Meanwhile, the control zebrafish maintained its swimming velocity and distance travelled throughout the three time-points, suggesting the effect of MPTP injection on zebrafish locomotor activity.
During the three-minute behaviour test, the freezing maintenance (duration and bouts) of the MPTP-injected zebrafish was higher and more frequent than the control zebrafish. MPTPinjected zebrafish spent more than two minutes in immobile condition 24h and 96h after injection ( Fig 5A). Notably, on the 24 th hour after injection, MPTP-injected zebrafish alternated between swimming and freezing more frequently, as evidenced by the increased number of freezing bouts ( Fig 5B).   The amount of time spent in the IN zone when compared to the OUT zone and the frequency with which it is visited is a type of swimming pattern that reflects the exploratory behaviour of a zebrafish. In our observation, although both the control and MPTP-injected zebrafish spent half of the time at the center of the assay tank and the other half circling the tank wall (Fig 6A), however, the MPTP-injected zebrafish appeared to switch between the center and the wall less frequently (Fig 6B), suggesting that they preferred to swim close to their initial position rather than exploring the surroundings.

PLOS ONE
Another factor to describe the swimming pattern of the zebrafish is the turning rate, which is defined as the speed at which the fish can turn and is studied by measuring three parameters: meander, angular velocity, and turn angle. The MPTP-injected zebrafish had greater turn angles at 24h and 96h after injection (30˚-40˚) than 0h and control zebrafish (*20˚) (Fig 7A). Corroborating this, the meander of MPTP-injected zebrafish, which is the change in direction of movement of a fish in relation to the distance moved by that fish, was three times greater at 24h and 96h after the injection than at 0h (Fig 7B), suggesting that the MPTP-injected fish turned at a greater degree per distance that it moved (˚/cm). Besides, the MPTP-injected zebrafish exhibited a higher angular velocity, as calculated by the change in direction of movement per unit time (˚/s). The rate of turn in direction of MPTP-injected zebrafish was nearly doubled 24h after injection and was increased by 50% on the 96th hour after injection when compared to 0h and control zebrafish (Fig 7C). Overall, MPTP-injected zebrafish had a higher turning rate 24h after injection and remained high 96 hours later.
Although a reduction in locomotor activity is the established hallmark for neurotoxininduced zebrafish neuropathic behaviour, the swimming phenotypes should also be

PLOS ONE
considered when interpreting zebrafish motor-related activity. From our observations, when compared to the control zebrafish, which exhibited normal continuous swimming, the MPTPinjected zebrafish exhibited abnormal swimming phenotypes, such as looping (distinct circular motion), freezing (complete movement cessation), and erratic movement (abrupt changes in velocity or direction as well as recurrent rapid darting) (Fig 8).
Despite the known regenerative ability of the zebrafish and the transient effect of MPTP neurotoxin on the zebrafish, we did not observe any tendency for the altered swimming behaviour to recover on the 96th hour after injection. Perhaps, a longer observation period is required for the recovery to show a discernible effect.

Changes in body weights after the administration of MPTP
Apart from the swimming behaviour, we also analysed the differences in the initial and final body weights of the experimental zebrafish. It is well known that experimental procedures, such as injection and prolonged isolation, may induce stress on zebrafish, leading to weight loss due to decreased appetite. Nevertheless, no significant difference was observed between the initial and final body weights of both MPTP-injected and control zebrafish (Fig 9).

Discussion
Emphasizing the induction of neurotoxin onto adult zebrafish to establish a reliable animal PD model, this study evaluated the effect of MPTP administration on the swimming behaviour of adult zebrafish. One dose of MPTP was delivered through i/p injection to adult zebrafish and its effects on swimming behaviour were examined in an open field test at three time points (0h, 24h, and 96h-post injection). The results of our study revealed that MPTP administration into adult zebrafish reduced the locomotor activity, altered the complexity of the swimming pattern, and induced abnormal swimming phenotypes. Besides that, the body weight changes in response to MPTP administration was investigated. Throughout the experimental period, we found that the body weights of both MPTP-injected and control zebrafish were unchanged.
Zebrafish is a well-known model for PD. The zebrafish ventral diencephalon (vDn) is thought to reflect the human substantia nigra since it is dominated by dopaminergic neurons. Furthermore, Du et al. [27] detected a dopaminergic projection from the vDn to the subpallium region in zebrafish larvae, suggesting that this projection is equivalent to the nigrostriatal dopaminergic pathway of humans. In terms of locomotion, zebrafish exhibit sophisticated behaviours reflective of PD. A number of studies have reported the effects of MPTP on zebrafish locomotion [18,19,21,25,30], but only a few have performed prolonged observation [21,25]. Assessing the behavioural changes at several time points is critical as it provides stronger evidence for the establishment of MPTP-induced zebrafish model of PD.
In this study, marked alterations in locomotor activity, indicated by slower swimming velocity, shorter distance travelled, and longer freezing maintenance, was detected 24 hours after the MPTP administration and still remained discernible 96 hours later. This implies that, compared to the control zebrafish, the MPTP-injected zebrafish swam slower and had periods of idleness. It is also fair to note that, the number of freezing bouts decreased from the 24th to the 96th hour following injection. This indicates that, on the 96 th hour, instead of alternating between swimming and freezing, the MPTP-injected zebrafish were predominantly immobile during the whole duration of the behavior test. Our finding is in line with those of previous studies, which documented hypolocomotion in neurotoxin-induced animal models [25,[28][29][30]. Anichtchik et al. [25] found a substantial decrease in locomotor activity and an increase in turn angle in MPTP-injected zebrafish on the 1 st , 3 rd , 6 th , and 9 th days following injection. However, the study lacks information on other swimming phenotypes such as meander and angular velocity. Furthermore, MPTP-injected zebrafish spent more time in the IN zone, according to the study. In contrast, we found that MPTP-injected and control zebrafish spent the same amount of time in the IN zone. The study did not, however, measure the number of crossings between the IN and OUT zones, which is more representative of the swimming pattern than time spent in the IN zone.
Aside from the locomotor activity, how the zebrafish swim is also a robust indicator of neurotoxic effects [31]. In this study, we observed that the swimming pattern of MPTP-injected zebrafish was different from that of control zebrafish. In terms of the time spent at the center of the tank, both groups showed similar duration, however, the control zebrafish crossed the center more frequently than the MPTP-injected zebrafish. An open field tank offers a new area for exploration [32]. In this context, a higher frequency of crossing the inner zone indicates zebrafish exploratory behaviour [33]. We interpreted that this reflects a regular swimming pattern. In contrast, the MPTP-injected zebrafish preferred to swim nearby their initial position and avoided frequent crossing of the center of the tank and remained in the same zone throughout the behaviour test period. Therefore, the tendency of the MPTP-injected zebrafish to stay in only one zone during the behavior test period suggests that the neurotoxin may have an effect on their exploratory behavior.
Another parameter that reflects the motor aspects of the zebrafish is the turning rate, which comprises of the turn angle, meander, and angular velocity. The turn angle is an important aspect in assessing fish behaviour as it is a measure of maneuverability achieved by muscular contraction of the tail [34]. Mechanically, the body must perform more work to navigate a larger turn angle [35]. Aside from being largely studied in the context of predatory or aversive stimuli, turn angle also corresponds with erratic movements [36]. In our study, MPTP-injected zebrafish had a slightly larger turn angle 24 hours after injection and a two-fold increase on the 96 th hour compared to controls. Meander on the other hand, measures the directionality of the fish [37]. Similar to the turn angle, a larger meander value is associated with erratic movements [32]. An increase in meandering was reported in adult zebrafish exposed to acute acrylamide [38] and mercury [39] neurotoxicity. Comparably, our MPTP-injected zebrafish had more than three times the meander values of controls at 24h and 96h post-injection, suggesting impaired directionality caused by MPTP neurotoxicity. Finally, when comparing MPTPinjected zebrafish to controls, we found that their angular velocity, or turning speed, was significantly higher. Most notably, after 96 hours following injection, the treated zebrafish had double the turning speed of controlled fish. Angular velocity, like meander, is used to assess the directionality of the fish [40]. Reportedly, a high angular velocity correlates to significant bending of zebrafish entire body, which reflects erratic movements [41,42]. Collectively, the turn angle, meander, and angular velocity of the zebrafish after MPTP administration were profoundly increased on the 24 th hour and kept increasing on the 96 th hour post-injection, resulting in fast and sharp changes in swimming direction. This behaviour could be analogous to the incoordination seen in human PD patients when executing voluntary movements. The cardinal motor features of PD include bradykinesia (slowness of movement) and impaired voluntary motor coordination [43] support the assertion that our zebrafish model of PD mimics human PD.
Most studies documented the path taken and the swimming speed, but they neglected to address the swimming phenotypes linked to neurotoxin-induced neuropathy. In our study, several different types of swimming were documented that were exclusively seen in the MPTPinjected group, but not in the control group, such as freezing, looping, and erratic movement. Freezing is characterized as a complete cessation of movement, except for gills and eyes [31]. MPTP-injected zebrafish in our study froze for the majority of the time throughout the behaviour test period. Notably, these zebrafish showed no signs of increased respiration, suggesting that the immobility was caused by the neurotoxic agent rather than stress or anxiety. Looping, on the other hand, is defined as a distinct circular motion [31]. Zebrafish is considered to be swimming in a loop when it is spinning around a virtual point outside the body, in contrast to circling which is characterized as an orbiting behaviour around a specific object or subject [31]. Repeated looping behaviour was observed in our MPTP-injected zebrafish, with a noticeable increase in velocity during the spinning motion. Looping behaviour in fish indicates uncontrolled movement due to motor impairment [31,44]. Looping is also associated with defective optic nerve projection which leads to visual system impairment [45]. Evidently, MPTP administration was found to cause retinal degeneration, a vital component that communicates with the optic nerve [17]. Apoptotic photoreceptors and inner retina neuronal loss were observed in mice treated with MPTP [17]. The optokinetic response (OKR) assay, which uses alternating dark and light concept, is particularly useful for assessing zebrafish visualmotor response and visual acuity [46]. Perhaps, this could account for the looping behaviour seen in our MPTP-injected zebrafish. However, in this study, we did not perform the OKR assay. Another abnormal swimming phenotype evident in the MPTP-injected zebrafish was erratic movement, which is defined as recurrent rapid darting with sharp directional changes [31]. This pattern of swimming indicates motor incoordination, which is usually associated with neurotoxicity [31,47].
In humans, the dopaminergic neuron in the SNpc modulates movement control through direct and indirect basal ganglia pathways [4]. Unfortunately, in PD, due to the significant dopaminergic neuronal loss, dopamine input from the SNpc is substantially reduced, and thus, disrupts the pathways. A transgenic mice model harboring the PD genotype showed diminished firing of nigral dopaminergic neurons and consequent loss of striatal dopamine signaling, resulting in movement impairment [48]. Likewise, MPTP has also been linked to the death of dopaminergic neurons. It has the ability to mimic the specific degeneration of nigral dopaminergic neurons seen in the development of PD. According to Sarath Babu et al. [18] and Selvaraj et al. [19], reduced locomotor activity in MPTP-induced animal models is comparable to human bradykinesia and dyskinesia, suggesting a disruption in motor control ability.
In terms of MPTP pharmacokinetics in zebrafish, intraperitoneally injected MPTP enters the zebrafish peritoneal cavity. Due to its small size (MW MPTP : 173.25 g/mol), MPTP is subsequently absorbed into the portal vein via mesenteric capillaries by diffusion. From the portal vein, it is transported to the brain through the circulatory system [49] and easily crosses the blood-brain barrier (BBB) [50]. Inside the brain, it is converted to MPP+ by monoamine oxidase B (MAO B), which is found in glial cells. The MPP+ is transported into dopaminergic neurons via dopamine transporter (DAT) protein due to its similar structure with dopamine [51][52][53]. The presence of MPP+ inside the dopaminergic neurons is toxic, as it impairs mitochondrial electron transport chain, leading to mitochondrial dysfunction [54], oxidative stress [55], neuroinflammation [56], and ultimately neuronal death. Conclusively, MPTP administration impairs movement control by degenerating dopaminergic neurons needed to modulate the movement pathways.
Kalyn & Ekker [21] reported a substantial reduction of dopaminergic neurons in the telencephalon and olfactory bulbs of adult zebrafish following MPTP treatment. Similarly, a rodent study by Alam et al. [57] documented a drop in nigral tyrosine hydroxylase (TH)-positive signals after MPTP induction, which indicates a reduction in dopaminergic neuronal density in the substantia nigra of MPTP-injected mice. Moreover, the same study detected a decrease in striatal dopamine concentrations, indicating a disruption in dopaminergic signaling between the substantia nigra and striatum regions of the treated mice [57]. Therefore, the alterations in swimming behaviours of the zebrafish observed in our study could be due to the dysregulation of the movement signaling pathway caused by MPTP-induced loss of dopaminergic neurons.
When assessing the effect of neurotoxin on animals, it is also useful to measure the difference between the final and initial body weights of the animals. It is well known that body weight loss is correlated with stress level [58]. Hence, information on the body weights may portray how stressful were the animals with the experimental regime. In our study, we found no significant differences in body weights before and after the experiment, indicating that both MPTP-injected and control zebrafish had normal appetites throughout the experimental period. This suggests that the i/p injection and the 96 hours isolation regime did not trigger stress in the zebrafish. Even so, further investigation should be carried out to support this claim, such as measuring the levels of stress hormone and the expression of stress-related genes.
While our data are preliminary, they imply that the time taken for MPTP neurotoxin to induce observable PD-like symptoms in adult zebrafish is around 24 hours after the intraperitoneal injection and the effect still persisted 96 th hour post-injection. This information is critical because most PD research utilizing MPTP-induced zebrafish model often aim to produce treatments or therapies that can potentially reduce or reverse PD symptoms. Hence, it is important to ensure that the MPTP effect is already stabilized, and persistent, otherwise confounding factors could skew the results and cause misinterpretation. Despite the known regenerative ability of the zebrafish and the transient effect of MPTP neurotoxin on the zebrafish, we did not observe any tendency for the altered swimming behaviour to recover on the 9 6t h hour after injection. Perhaps, a longer observation period is required for the recovery to show a discernible effect. Also, a recent study delivered MPTP neurotoxin into adult zebrafish through intracerebroventricular (icv) injection and reported hypolocomotion effect [21]. It is fair to note that, our findings corroborate the observation seen in their study, demonstrating that the i/p injection technique is comparable to the more advanced icv injection technique.
Our study focused solely on the behavioural aspect of MPTP on adult zebrafish. Future works will include correlating the behavioural profile with molecular aspects, such as genomic and proteomic networking, as well as histochemical changes in the brain of MPTP-injected zebrafish, to obtain more sophisticated information on how MPTP actions on the brain translate into behavioural presentations. Also, we observed the behaviour only at three time points (0h, 24h, and 96h post-injection). To observe more gradual changes and long-term MPTP effect, smaller time intervals (for example, 12-hourly) and longer observation of the behaviour test should be conducted. Plus, further work can be done to compare the swimming behaviour between male and female zebrafish to study sex differences on MPTP-induced locomotor impairment. Notwithstanding these limitations, our study offers some insights into the swimming behaviour, in terms of locomotor activity and swimming pattern, of the MPTP-induced zebrafish model of PD.

Conclusions
Taken together, our findings demonstrate that a single systemic injection of MPTP (200 μg/g bw) into adult zebrafish causes significant reduction in locomotor activity, changes in swimming pattern, and abnormal swimming phenotypes, but no significant body weight changes.
One of the more significant conclusions to emerge from this study is that MPTP effects on adult zebrafish can be distinctively seen after 24 hours of its administration and still persisted 96 hours later. The second key conclusion is that, in addition to decreased locomotor activity, MPTP administration provoked motor incoordination in adult zebrafish, as seen by the complexity of swimming pattern and abnormal swimming phenotypes in MPTP-injected zebrafish. Further investigations are needed to determine the MPTP mechanism of action that causes these changes.